| Tag | Content |
|---|
EnhancerAtlas ID | HS120-01971 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr14:100275670-100276840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr14:100276618-100276636 | CATGGGTTCCTTCCTTCC | - | 6.3 | | EWSR1-FLI1 | MA0149.1 | chr14:100276622-100276640 | GGTTCCTTCCTTCCTTCA | - | 6.83 | | EWSR1-FLI1 | MA0149.1 | chr14:100276626-100276644 | CCTTCCTTCCTTCATTTC | - | 7.97 | | NFAT5 | MA0606.1 | chr14:100275780-100275790 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr14:100275780-100275790 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr14:100275780-100275790 | ATTTTCCATT | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_04526 | chr14:100275585-100276859 | Brain_Anterior_Caudate |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I099808 | chr14 | 100275084 | 100277035 |
|
Enhancer Sequence | TTTTATTTAT TTATTTATTT AATTCCTCTT CTCCCTCAAA GCACAATCTG CTGTATGTTA 60
AAGGGGCGGG GAAGCTGCTG ACTTTGCAGT AGCGCATACT TACTCACGCA ATTTTCCATT 120
CTGGCTGAAG TAAGGGATGA GACAGCATGC CCAGAAGCTG TGTCCAGCAC TTGGACAGGC 180
GCCCTGGTCG GCACCCTGGG AACCTCGGCC GTGCACTGCC AGCTTTCTGG GTCCATCCCA 240
GCCCTGGGTG TATGGCAGAT GCCTTGAGAT TTAACAGCCC TTGAGTCAGG CCTGCAACGT 300
CTTATCTGCG ATTTCAACAT CCAGAAAGCT GTGAAACCCA GATGTTTTTT GGTAACTTGT 360
TTGCTAGTTG GATTTGGCCT GATCTGAAAT CATTTGATGG GTGGGGAGAA CTCCTCTGAA 420
TTGAAACATG TGGCTTTTAA TCGTTTGTGT TCATTTCTTT TAGTGTGAAA GTTCTGCTTT 480
TCTGTAGAGG TATTTTTGAA TGTGACTATG GGTCTTGTCC TAGGCCCTTC TGGGATATTG 540
GCTAATGTAT GGTGTATGCC CTGGACTTCC GTTTTAAAGT CTGAATCTGA GTTCAAAAAC 600
ATTTCAGGCC CCAGGGATTT GAGGAAGGGT TTCCAGACCA GTATAACCAG ACAGCCGAGC 660
CGGCCCTGTA CCGCGTCTGG TTCCTGGGTG GTTCCTGCTG CAATGCGGCC CAGTCAGGGC 720
ACTGCTGCTG ACTTGTATCT GCGGACACTC CCCAGTGTTT GAGTGATGTT TACGTGGAAG 780
CCTGGCGTGT AGGAAGCTGG CGCCCCTGGG GGAACTGCAA GGCCATTTTA CAGCATTCAC 840
CTGTCACCGT GTCCTTCAGA ACCAGCCAGA TGCTACAGAG CCAGGCTGTA CCAGAGTCCA 900
GGCCCATGAA AACAAAGTTC AGGGAGACTC TGTTGACTTT GCTAAATTCA TGGGTTCCTT 960
CCTTCCTTCA TTTCTTTGTT CAACAGGAAT TTATGTATCT GCCATAAGAA GACCTGTGCT 1020
TGGCTTGTGA AAAGTAGCAG TGACACTTCA CATGAGTGTA ACATCTGCGG TTTATGGTTT 1080
TGTTGCAGTG TTTCATTTCG TCCTCGCAAC CATTCAGTGG ACCAGCTGGT GTTGGCCCTT 1140
TTCATAGATG AGGAAACTGA GGGCTAAATA 1170
|
